Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs1445846

ZNF354C

rs1445846 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF354C. Location: chromosome 5, position 178,507,069. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

ZNF354CNot classified
Variant type
missense_variant
Chromosome / position
5:178507069
HGVS
NM_014594.3,c.1636T>C,p.Phe546Leu
Allele change
Missense_F546L

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.